K-number	K011221
Device name	PRISMA HF 1000 SET, PRISMA HF 1000 PRE-SET
Applicant	Gambro Renal Products
Product code	KDI
Device class	Class II
Decision date	Oct 31, 2001
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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PRISMA HF 1000 SET, PRISMA HF 1000 PRE-SET

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